Chronic Epstein-Barr virus infection syndrome
Synonyms: CAEBV syndrome · Chronic EBV infection syndrome
- Type
- Disease
- Group
- Disorder
- Inheritance
- Unknown
- Age of onset
- Adolescent, Adult, Childhood
- Status
- active
Chronic Epstein-Barr virus infection syndrome is a rare infectious disease characterized by familial, primary, chronic Epstein-Barr virus infection which typically manifests with persistent mononucleosis-like signs and symptoms, in the absence of secondary immunodeficiency.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Chronic Epstein-Barr virus infection syndrome | CAEBV syndrome · Chronic EBV infection syndrome |
| fr | Syndrome d'infection chronique au virus Epstein-Barr | Syndrome CAEBV · Syndrome d'infection chronique à EBV |
| de | Ebstein-Barr-Virusinfektion, chronische | CAEBV-Syndrom · EBV-Infektion, chronische |
| es | Síndrome de infección crónica por el virus de Epstein-Barr | Síndrome CAEBV · Síndrome de infección crónica por EBV |
| it | Sindrome da infezione cronica da virus di Epstein-Barr | |
| nl | Chronische infectie met Epstein-Barrvirus-syndroom | CAEBV-syndroom · Chronische EBV-infectie-syndroom |
| pt | Síndrome de infeção crónica por vírus de Epstein-Barr | Síndrome CAEBV · Síndrome de infeção EBV crónica |
| pl | Zespół przewlekłego zakażenia wirusem Epsteina i Barr | = en |
| cs | Chronická EBV infekce | CAEBV syndrom · Syndrom chronické EBV infekce |
| uk | Синдром хронічної вірусної інфекції Епштейна-Барр | Синдром CAEBV · Синдром хронічної EBV-інфекції |
| zh | 慢性EB病毒感染综合征 | 慢性EB病毒感染综合征 |
| tr | Kronik Epstein-Barr virüs enfeksiyonu sendromu | CAEBV sendromu · Kronik EBV enfeksiyon sendromu |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 226990 | E | validated | |
| ICD-10 | B27.0 | NTBT | attributed | validated |
| ICD-11 | 1D81.0 | NTBT | attributed | validated |
| MONDO | 0009194 | E | validated | |
| UMLS | C4751209 | E | validated | |
| GARD | 9534 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:163585Rare viral disease
rare infectious diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Validated | ORPHANET_21348109[PMID] |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/2566
- This record as JSON: /data/d/2566.json